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Loss of tyrosinase activity confers increased skin tumor susceptibility in mice

TitleLoss of tyrosinase activity confers increased skin tumor susceptibility in mice
Publication TypeArticolo su Rivista peer-reviewed
Year of Publication2004
AuthorsSaran, Anna, Spinola M., Pazzaglia Simonetta, Peissel B., Tiveron C., Tatangelo L., Mancuso Mariateresa, Covelli V., Giovannelli L., Pitozzi V., Pignatiello C., Milani S., Dolara P., and Dragani T.A.
Keywordsalbinism, allele, animal, animal cell, animal model, Animalia, Animals, article, cancer cell culture, carcinogenesis, controlled study, dimethylbenz[a]anthracene, DNA damage, enzyme activity, enzymology, Gene expression, gene mutation, genetic predisposition, Genetic Predisposition to Disease, genetic susceptibility, genetics, Hydrogen Peroxide, metabolism, Mice, monophenol monooxygenase, mouse, Mus musculus, nonhuman, oxidation reduction reaction, Oxidation-Reduction, priority journal, Skin Neoplasms, skin papilloma, skin tumor, squamous cell carcinoma, systematic review, Transgenic, transgenic mouse, tyrosine

The tyrosinase (Tyr) gene encodes the enzyme tyrosinase that catalyses the conversion of L-tyrosine into DOPA (3,4-dihydroxypheaylalanine)-quinone. The albino mutation abrogates functional activity of tyrosinase resulting in deficiency of melanin pigment production in skin and retina. Tyr maps to a region in the central position of Chromosome 7 that contains a skin tumor-modifier locus. We rescued the albino mutation in transgenic mice to assess a possible role of Tyr gene in two-stage skin carcinogenesis. Transgenic expression of the functional TyrCys allele in albino mice (Tyr Ser) caused a reduction in skin papilloma multiplicity, in four independent experiments and at three dose levels of DMBA (9,10-dimethyl-1,2- benzanthracene). In vitro mechanistic studies demonstrated that transfection of the TyrCys allele in a human squamous cell carcinoma cell line (NCI-H520) increases tyrosinase enzyme activity and confers resistance to hydrogen peroxide-induced oxidative DNA damage. These results provide direct evidence that the Tyr gene can act as a skin cancer-modifier gene, whose mechanism of action may involve modulation of oxidative DNA damage.


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Citation KeySaran20044130